Variant report

Variant rs61839803
Chromosome Location chr1:246621278-246621279
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246602000-246622800 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr1:246611200-246625000 Weak transcription Osteobl bone
3 chr1:246614000-246625600 Weak transcription Fetal Kidney kidney
4 chr1:246618000-246623400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:246619000-246639600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:246619800-246624000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:246619800-246624200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:246621000-246622600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr1:246621000-246622800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr1:246621200-246621400 Enhancers Primary hematopoietic stem cells blood
11 chr1:246621200-246621600 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr1:246621200-246621600 Enhancers Fetal Heart heart
13 chr1:246621200-246621600 Enhancers HUVEC blood vessel

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